ClearanceBrief
510(k) K844173 ยท HES Insufflator, Carbon-Dioxide, Uterotubal (And Accessories)

FEMTEST

ApplicantBionexus, Inc., Raleigh NC, US
DecisionSubstantially Equivalent, Aug 14, 1985
ReceivedOct 25, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K844173

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.